Teduglutide
ATC A16AX08 · 6 markets · 12 records
AU 5 records · 2 strengths
- 5 mginjectionCIPLA TEDUGLUTIDE teduglutide 5 mg powder for injection vial with diluent prefilled syringe kitDENOLOC teduglutide 5 mg powder for injection vial with diluent prefilled syringe kit、REVESTIVE、REVESTIVE teduglutide 5 mg powder for solution for injection vial with diluent pre-filled syringe
Records without a stated strength · 1 REVESTIVE
GB 2 records · 2 strengths
EU 2 records · 1 strengths
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Records without a stated strength · 1 REVESTIVE、Teduglutide Viatris
US 1 records · 1 strengths
- 5 mg/0.5 mLinjectionGattex
CA 1 records · 1 strengths
- 5 mgliquidREVESTIVE
TW 1 records · 1 strengths
- 5 mginjectionREVESTIVE利腸服5毫克注射劑
| Strength / form / release | US | GB | CA | AU | TW | EU |
|---|---|---|---|---|---|---|
| 5 mg injection | Revestive 5mg powder and solvent for solution for injection vials | CIPLA TEDUGLUTIDE teduglutide 5 mg powder for injection vial with diluent prefilled syringe kit DENOLOC teduglutide 5 mg powder for injection vial with diluent prefilled syringe kit REVESTIVE+1REVESTIVE teduglutide 5 mg powder for solution for injection vial with diluent pre-filled syringe | REVESTIVE 利腸服5毫克注射劑 | |||
| 5 mg liquid | REVESTIVE | |||||
| 5 mg/0.5 mL injection | Gattex | |||||
| 1.25 mg injection | Revestive 5mg powder and solvent for solution for injection vials | |||||
unknown | REVESTIVE | REVESTIVE Teduglutide Viatris |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in CA and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en CA que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 CA 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 CA 有記錄(未在本表顯示)。
“not disclosed” means the source does not publish the strength — it does not mean the product has none.
Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.